Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation
Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor composed of histologically and immunohistochemically distinctive perivascular epithelioid cells (PECs). Both benign and malignant tumors have been identified, but the criteria for diagnosis of malignancy have not been fully est...
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doaj-512e6d642c3247239455aefb3570b44e2020-11-24T22:44:31ZengElsevierHematology/Oncology and Stem Cell Therapy1658-38762009-07-0123426430Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentationJing-Lan Liu0Yueh-Min Lin1Ming-Chieh Lin2Kun-Tu Yeh3Jui- Chang Hsu4Chih-Jung Chen5Changhua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaCorrespondence: Chih-Jung Chen · Changhua Christian Hospital, Changhua, Taiwan, Province of China; Changhua Christian Hospital, Changhua, Taiwan, Province of ChinaPerivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor composed of histologically and immunohistochemically distinctive perivascular epithelioid cells (PECs). Both benign and malignant tumors have been identified, but the criteria for diagnosis of malignancy have not been fully established due to the rarity of the tumor. We report on a case of uterine PEComa in a 33-year old woman with lymph node metastasis at presentation. The tumor had the characteristic histologic features of PEComa with cytologic atypia, mitotic activity of 2/10 high power field (HPF), and necrosis; it exhibited im-munopositivity for HMB-45, calponin and desmin and was negative for melan-A. The patient received neoadjuvant chemotherapy, debulking surgery and adjuvant chemotherapy. No evidence of recurrence or metastasis was apparent 8 months after surgery.http://www.sciencedirect.com/science/article/pii/S1658387609500131 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jing-Lan Liu Yueh-Min Lin Ming-Chieh Lin Kun-Tu Yeh Jui- Chang Hsu Chih-Jung Chen |
spellingShingle |
Jing-Lan Liu Yueh-Min Lin Ming-Chieh Lin Kun-Tu Yeh Jui- Chang Hsu Chih-Jung Chen Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation Hematology/Oncology and Stem Cell Therapy |
author_facet |
Jing-Lan Liu Yueh-Min Lin Ming-Chieh Lin Kun-Tu Yeh Jui- Chang Hsu Chih-Jung Chen |
author_sort |
Jing-Lan Liu |
title |
Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation |
title_short |
Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation |
title_full |
Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation |
title_fullStr |
Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation |
title_full_unstemmed |
Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation |
title_sort |
perivascular epithelioid cell tumor (pecoma) of the uterus with aggressive behavior at presentation |
publisher |
Elsevier |
series |
Hematology/Oncology and Stem Cell Therapy |
issn |
1658-3876 |
publishDate |
2009-07-01 |
description |
Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor composed of histologically and immunohistochemically distinctive perivascular epithelioid cells (PECs). Both benign and malignant tumors have been identified, but the criteria for diagnosis of malignancy have not been fully established due to the rarity of the tumor. We report on a case of uterine PEComa in a 33-year old woman with lymph node metastasis at presentation. The tumor had the characteristic histologic features of PEComa with cytologic atypia, mitotic activity of 2/10 high power field (HPF), and necrosis; it exhibited im-munopositivity for HMB-45, calponin and desmin and was negative for melan-A. The patient received neoadjuvant chemotherapy, debulking surgery and adjuvant chemotherapy. No evidence of recurrence or metastasis was apparent 8 months after surgery. |
url |
http://www.sciencedirect.com/science/article/pii/S1658387609500131 |
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